» Articles » PMID: 32015352

RNA-Seq Reveals Novel Genes and Pathways Associated with Hypoxia Duration and Tolerance in Tomato Root

Overview
Journal Sci Rep
Specialty Science
Date 2020 Feb 5
PMID 32015352
Citations 28
Authors
Affiliations
Soon will be listed here.
Abstract

Due to climate change, economically important crop plants will encounter flooding periods causing hypoxic stress more frequently. This may lead to reduced yields and endanger food security. As roots are the first organ to be affected by hypoxia, the ability to sense and respond to hypoxic stress is crucial. At the molecular level, therefore, fine-tuning the regulation of gene expression in the root is essential for hypoxia tolerance. Using an RNA-Seq approach, we investigated transcriptome modulation in tomato roots of the cultivar 'Moneymaker', in response to short- (6 h) and long-term (48 h) hypoxia. Hypoxia duration appeared to have a significant impact on gene expression such that the roots of five weeks old tomato plants showed a distinct time-dependent transcriptome response. We observed expression changes in 267 and 1421 genes under short- and long-term hypoxia, respectively. Among these, 243 genes experienced changed expression at both time points. We identified tomato genes with a potential role in aerenchyma formation which facilitates oxygen transport and may act as an escape mechanism enabling hypoxia tolerance. Moreover, we identified differentially regulated genes related to carbon and amino acid metabolism and redox homeostasis. Of particular interest were the differentially regulated transcription factors, which act as master regulators of downstream target genes involved in responses to short and/or long-term hypoxia. Our data suggest a temporal metabolic and anatomic adjustment to hypoxia in tomato root which requires further investigation. We propose that the regulated genes identified in this study are good candidates for further studies regarding hypoxia tolerance in tomato or other crops.

Citing Articles

Comparative Transcriptome Analyses Reveal the Mechanisms Underlying Waterlogging Tolerance in Barley.

Zhu J, Yin H, Cao C, Sun C, Zhang M, Hong Y Plants (Basel). 2025; 14(1.

PMID: 39795288 PMC: 11722848. DOI: 10.3390/plants14010028.


Harnessing transcriptome sequencing to identify and characterize genes regulating carbohydrate biosynthesis pathways in L.

Abbas Z, Al-Huqail A, Abdel Kawy A, Abdulhai R, Albalawi D, Alshaqhaa M Front Plant Sci. 2024; 15:1467432.

PMID: 39391775 PMC: 11464306. DOI: 10.3389/fpls.2024.1467432.


Hypoxia increases triacylglycerol levels and unsaturation in tomato roots.

Striesow J, Welle M, Busch L, Bekeschus S, Wende K, Stohr C BMC Plant Biol. 2024; 24(1):909.

PMID: 39350052 PMC: 11441241. DOI: 10.1186/s12870-024-05578-4.


Transcriptomic analysis reveals the regulatory mechanisms of messenger RNA (mRNA) and long non-coding RNA (lncRNA) in response to waterlogging stress in rye (Secale cereale L.).

Bimpong D, Zhao L, Ran M, Zhao X, Wu C, Li Z BMC Plant Biol. 2024; 24(1):534.

PMID: 38862913 PMC: 11167852. DOI: 10.1186/s12870-024-05234-x.


Omics-driven exploration and mining of key functional genes for the improvement of food and fiber crops.

Naqvi R, Mahmood M, Mansoor S, Amin I, Asif M Front Plant Sci. 2024; 14:1273859.

PMID: 38259913 PMC: 10800452. DOI: 10.3389/fpls.2023.1273859.


References
1.
Bailey-Serres J, Voesenek L . Flooding stress: acclimations and genetic diversity. Annu Rev Plant Biol. 2008; 59:313-39. DOI: 10.1146/annurev.arplant.59.032607.092752. View

2.
Dordas C, Hasinoff B, Igamberdiev A, Manach N, Rivoal J, Hill R . Expression of a stress-induced hemoglobin affects NO levels produced by alfalfa root cultures under hypoxic stress. Plant J. 2003; 35(6):763-70. DOI: 10.1046/j.1365-313x.2003.01846.x. View

3.
Liu P, Sun F, Gao R, Dong H . RAP2.6L overexpression delays waterlogging induced premature senescence by increasing stomatal closure more than antioxidant enzyme activity. Plant Mol Biol. 2012; 79(6):609-22. DOI: 10.1007/s11103-012-9936-8. View

4.
Weits D, Giuntoli B, Kosmacz M, Parlanti S, Hubberten H, Riegler H . Plant cysteine oxidases control the oxygen-dependent branch of the N-end-rule pathway. Nat Commun. 2014; 5:3425. PMC: 3959200. DOI: 10.1038/ncomms4425. View

5.
Schmittgen T, Livak K . Analyzing real-time PCR data by the comparative C(T) method. Nat Protoc. 2008; 3(6):1101-8. DOI: 10.1038/nprot.2008.73. View